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Fig 1.

Identification of the RBITC-labeled chitosan.

(A) Scheme of synthesis of the RBITC-labeled chitosan. (B) FTIR spectra of the unlabeled and RBITC-labeled chitosan.

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Fig 2.

Characterization of unlabeled and RBITC-labeled TmCS-NPs.

(A) Particle size, PDI, and zeta potential of the unlabeled and RBITC-labeled TmCS-NPs. (B) TEM analysis of the TmCS-NPs. (C) Particle size graphs of TmCS-NPs and RBITC-labeled TmCS-NPs. (D) Zeta potential graphs of TmCS-NPs and RBITC-labeled TmCS-NPs.

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Fig 2 Expand

Fig 3.

(A) Ex-vivo fluorescence images of the brains with RBITC-labeled TmCS-NPs after systemic injection at 0.5, 2, 4, 8, and 24 h. (B) Fluorescence photographs of the sub-brain regions separated from the brains above at 0.5, 2, 4, 8, and 24 h.

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Fig 3 Expand

Fig 4.

Changes in the GSH, H2O2, and MDA levels in the frontal cortex and cerebellum of rats (n = 6, six rats per group) intravenously injected with physiological saline (control) and TmCS-NPs (3, 10, and 30 mg/kg) for 7 d.

(A, B, and C) GSH, H2O2, and MDA levels in the frontal cortex, respectively; (D, E, and F) GSH, H2O2, and MDA levels in the cerebellum, respectively. *p < 0.05 when compared with the control group.

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Fig 4 Expand

Fig 5.

Body weight changes in rats (n = 6, six rats per group) intravenously injected with physiological saline (control) and TmCS-NPs (3, 10, and 30 mg/kg) for 7 d.

*p < 0.05 when compared with the control group. #p < 0.01 when compared with the control group.

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Fig 5 Expand

Fig 6.

Histopathology of the rat brain tissue after intravenous injection with physiological saline (control) and TmCS-NPs (3, 10, and 30 mg/kg) for 7 d.

(A) Frontal cortex region; (B) Frontal cortex region of the middle-dose group. (C) Cerebellum region.

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Fig 6 Expand

Fig 7.

Immunohistological staining of the GFAP and NeuN of the rat brain tissue after intravenous injection with physiological saline (control) and TmCS-NPs (3, 10, and 30 mg/kg) for 7 d.

(A) GFAP expression in the frontal cortex region; (A’) Semi-quantification analysis of the GFAP expression in the frontal cortex. (B) GFAP expression in the cerebellum region; (B’) Semi-quantification analysis of the GFAP expression in the cerebellum. (C) NeuN expression in the frontal cortex region; and (D) NeuN expression in the cerebellum region. *p < 0.05 when compared with the control group, #p < 0.01 when compared with the control group.

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Fig 7 Expand